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On-site gmp document control lead & technical writer

Amgen Sa
Document controller
Posted: 2 April
Offer description

A leading biotechnology company in Dún Laoghaire, Ireland, is seeking a Senior Document Control Associate.
This role involves managing change controls and updating operational documentation while ensuring compliance with GMP standards.
The ideal candidate should possess strong technical writing skills, project management capabilities, and a Bachelor's degree in a relevant discipline.
Additionally, candidates need experience in a cGMP environment and the ability to manage multiple priorities in a fast-paced setting.
This position predominantly requires on-site attendance.
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